Skip to content
  • Pharma Tips
  • Pharma GMP
  • Pharma SOP
  • Pharma Books
  • Schedule M

StabilityStudies.in

Pharma Stability: Insights, Guidelines, and Expertise

Tag: Stability testing

How to Conduct Stability Studies for Drugs with Complex API in Compliance with Regulatory Guidelines

Posted on By

How to Conduct Stability Studies for Drugs with Complex API in Compliance with Regulatory Guidelines Stability Testing for Drugs with Complex APIs: A Regulatory Compliance Guide Introduction Drugs with complex Active Pharmaceutical Ingredients (APIs), such as peptides, proteins, and other large molecules, pose unique challenges in stability testing due to their susceptibility to degradation and…

Read More “How to Conduct Stability Studies for Drugs with Complex API in Compliance with Regulatory Guidelines” »

'How to' - Stability Studies

SOP for Performing Humidity Chamber Studies for Drug Products

Posted on By

SOP for Performing Humidity Chamber Studies for Drug Products Procedure for Conducting Humidity Chamber Studies on Drug Products 1) Purpose The purpose of this SOP is to provide a standardized procedure for performing humidity chamber studies to evaluate the stability of drug products under various humidity conditions. 2) Scope This SOP applies to all drug…

Read More “SOP for Performing Humidity Chamber Studies for Drug Products” »

Stability Studies SOP

How to Apply ICH Q10 for Pharmaceutical Quality System in Stability Studies

Posted on By

How to Apply ICH Q10 for Pharmaceutical Quality System in Stability Studies Applying ICH Q10 for Stability Studies: Enhancing Pharmaceutical Quality Systems Introduction ICH Q10, the Pharmaceutical Quality System guideline, provides a comprehensive framework for maintaining and improving the quality of pharmaceutical products throughout their lifecycle. Applying ICH Q10 principles to stability studies helps ensure…

Read More “How to Apply ICH Q10 for Pharmaceutical Quality System in Stability Studies” »

'How to' - Stability Studies

How to Conduct Stability Testing for Modified-Release Formulations in Compliance with Regulatory Guidelines

Posted on By

How to Conduct Stability Testing for Modified-Release Formulations in Compliance with Regulatory Guidelines Stability Testing for Modified-Release Formulations: Ensuring Regulatory Compliance Introduction Modified-release formulations, such as extended-release, delayed-release, and controlled-release products, are designed to release their active ingredients over a specific period. Stability testing for these formulations is critical to ensure they maintain their intended…

Read More “How to Conduct Stability Testing for Modified-Release Formulations in Compliance with Regulatory Guidelines” »

'How to' - Stability Studies

How to Implement ICH Q8 for Stability Testing in Pharmaceutical Development

Posted on By

How to Implement ICH Q8 for Stability Testing in Pharmaceutical Development Applying ICH Q8 for Stability Testing in Pharmaceutical Development Introduction The ICH Q8 guideline, “Pharmaceutical Development,” emphasizes a systematic approach to development that ensures product quality through design, understanding, and control of manufacturing processes. Implementing ICH Q8 principles in stability testing helps to optimize…

Read More “How to Implement ICH Q8 for Stability Testing in Pharmaceutical Development” »

'How to' - Stability Studies

SOP for Conducting Photostability Testing of Drug Products

Posted on By

SOP for Conducting Photostability Testing of Drug Products Procedure for Photostability Testing of Drug Products 1) Purpose The purpose of this SOP is to provide a detailed procedure for conducting photostability testing of drug products to evaluate their stability when exposed to light, in order to determine suitable packaging and storage conditions. 2) Scope This…

Read More “SOP for Conducting Photostability Testing of Drug Products” »

Stability Studies SOP

How to Prepare Stability Data for Compliance with FDA’s Quality by Design (QbD) Approach

Posted on By

How to Prepare Stability Data for Compliance with FDA’s Quality by Design (QbD) Approach Stability Data Preparation for Compliance with FDA’s QbD Approach Introduction The FDA’s Quality by Design (QbD) approach emphasizes building quality into pharmaceutical products through a systematic understanding of processes and product characteristics. Preparing stability data under the QbD framework involves integrating…

Read More “How to Prepare Stability Data for Compliance with FDA’s Quality by Design (QbD) Approach” »

'How to' - Stability Studies

How to Conduct Stability Studies for Dermatological Products in Compliance with Regulatory Guidelines

Posted on By

How to Conduct Stability Studies for Dermatological Products in Compliance with Regulatory Guidelines Stability Testing for Dermatological Products: A Regulatory Guide Introduction Dermatological products, including creams, ointments, gels, and lotions, require specific stability testing to ensure their safety, efficacy, and quality. These products are often sensitive to environmental factors such as light, temperature, and humidity,…

Read More “How to Conduct Stability Studies for Dermatological Products in Compliance with Regulatory Guidelines” »

'How to' - Stability Studies

How to Implement Stability Studies for Drug Products in Multi-Layered Packaging under Regulatory Guidelines

Posted on By

How to Implement Stability Studies for Drug Products in Multi-Layered Packaging under Regulatory Guidelines Stability Testing for Drug Products in Multi-Layered Packaging: Regulatory Compliance Guide Introduction Drug products in multi-layered packaging, such as blister packs or pouches, require specific stability testing to ensure their safety, efficacy, and quality throughout their shelf life. Multi-layered packaging can…

Read More “How to Implement Stability Studies for Drug Products in Multi-Layered Packaging under Regulatory Guidelines” »

'How to' - Stability Studies

SOP for Determining the Impact of Temperature on Drug Stability

Posted on By

SOP for Determining the Impact of Temperature on Drug Stability Procedure for Evaluating the Effect of Temperature on Drug Stability 1) Purpose The purpose of this SOP is to provide a detailed procedure for determining the impact of temperature on the stability of drug substances and products. This evaluation helps in understanding the effects of…

Read More “SOP for Determining the Impact of Temperature on Drug Stability” »

Stability Studies SOP

Posts pagination

Previous 1 … 30 31 32 … 52 Next

Quick Guide

  • Stability Tutorials
  • Types of Stability Studies
  • Stability Studies SOP
  • ‘How to’ – Stability Studies
  • Regulatory Guidelines
  • Shelf Life and Expiry Dating
  • Stability Documentation
  • Stability Studies – API
  • Stability Studies Blog
  • Stability Studies FAQ
  • Packaging – Containers – Closers

    more

    Copyright © 2025 StabilityStudies.in.

    Powered by PressBook WordPress theme